BENEFITS n All database log dates were successfully achieved for all clinical studies and final data transferred to the client ahead of their expected timelines n The client successfully met their regulatory submission deadlines without delay NEED n For multiple international Phase I and III studies over a one-year period, more than 140,000 samples required PK and/or ADA sample analysis n Database log date was two weeks after last sample arrival, additionally PK samples of each subject had to be analyzed within the same analytical run APPROACH n Developed a flexible, global scheduling approach within the client’s respective time window to ensure the availability of scientists to perform the required assays n Effective communication with associated Centr

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